Associate Director, Statistical Programming

Contact name: Emily Munn

Contact email: emily.munn@medella.life
Job ref: 544
Published: over 1 year ago
One of our best clients, a small global CRO specializing in the management and analysis of clinical data, is seeking an Associate Director of Statistical Programming to join their team.


The role:
  • Provide leadership/expertise in resolving complex problems in support of division/company objectives, assigned projects, or as a consultant to others.
  • Represent the company and the statistical programming department in customer development and liaison.
  • Lead assigned projects by applying management skills and regulatory standards and requirements.
  • Allocate workload and resources according to study/project needs.
  • Ensure quality control and quality assurance by overseeing study teams’ work and meeting with the study teams on a one-on-one basis.
  • Monitor timelines for programming area activities for assigned projects.
  • Develop training matrix and coordinate and schedule technical training and SOP training through monthly programmer meeting.
  • Provide statistical programming support to assigned studies.
  • Develop and maintain clinical trial data and statistical reporting standards in line with pharmaceutical industry standards and conventions.
  • Assist in developing statistical programming Standard Operating Procedures and guidelines.
  • Develop and implement statistical programming good working practices.
  • Assist in recruiting and developing of statistical programmers.
  • Provide technical training to programmers and biostatisticians.

About you:
  • BS or higher degree in Computer Science, Biostatistics, Mathematics or related field.
  • 8 years of experience in statistical programming in the pharmaceutical industry.